HCID 22252364, compound → HCID 17908964, compound

HRID 1611982Notes

Reaction equation

HRID 1611982 reaction equation
[C:1]1([NH:7][C:8]2[CH:13]=[C:12]([O:14][CH3:15])[C:11]([O:16][CH3:17])=[C:10]([O:18][CH3:19])[CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20]1[N:25]([CH2:26][CH2:27][CH2:28][C:29](O)=[O:30])[CH2:24][CH2:23][N:22]2[CH2:32][CH2:33][CH2:34][CH2:35][CH:21]12>>[C:1]1([N:7]([C:8]2[CH:13]=[C:12]([O:14][CH3:15])[C:11]([O:16][CH3:17])=[C:10]([O:18][CH3:19])[CH:9]=2)[C:29](=[O:30])[CH2:28][CH2:27][CH2:26][N:25]2[CH2:24][CH2:23][N:22]3[CH2:32][CH2:33][CH2:34][CH2:35][CH:21]3[CH2:20]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

3

Reactant 2

HCID 22252364HCID 22252364, compoundHCID 22252385HCID 22252385, compound

Product 1

HCID 17908964HCID 17908964, compound

Procedure

The procedure is as for Example 2 using as substrate phenyl-(3,4,5-trimethoxyphenyl)amine and the compound obtained in Step B of Example 2.

Sources & evidence

ORD record
ord-4b77359fa25047a8803fce3d5ae6d785
Source dataset
uspto-grants-2006_01
Patent number
US06992085B2

Reaction notes

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